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海兔感觉神经元中5-羟色胺调节作用的药理学解离

Pharmacological dissociation of modulatory effects of serotonin in Aplysia sensory neurons.

作者信息

Mercer A R, Emptage N J, Carew T J

机构信息

Yale University, Department of Psychology, New Haven, CT 06520.

出版信息

Science. 1991 Dec 20;254(5039):1811-3. doi: 10.1126/science.1662413.

Abstract

In the mollusk Aplysia the neurotransmitter serotonin (5HT) has a fundamental modulatory role in several forms of learning and memory that involve an increase in the efficacy of synaptic transmission between tail sensory neurons (SNs) and motor neurons. The classical 5HT antagonist cyproheptadine (CYP) permits dissociation of three forms of serotonergic modulation in these SNs: (i) CYP reversibly blocks spike-broadening induced either by exogenous application of 5HT or by sensitizing stimulation of a tail nerve. (ii) CYP does not block 5HT-induced or tail input-induced increases in SN somatic excitability. (iii) Concomitant with its block of spike-broadening, CYP reversibly blocks 5HT-induced facilitation of synaptic transmission from SNs. These results suggest that endogenously released 5HT may act at different receptor subtypes that are coupled to different forms of neuromodulation in tail SNs of Aplysia.

摘要

在软体动物海兔中,神经递质5-羟色胺(5HT)在几种学习和记忆形式中具有重要的调节作用,这些学习和记忆形式涉及尾部感觉神经元(SNs)和运动神经元之间突触传递效率的提高。经典的5HT拮抗剂赛庚啶(CYP)能够分离这些SNs中三种形式的5-羟色胺能调节:(i)CYP可逆地阻断由外源性应用5HT或尾部神经的致敏刺激诱导的动作电位展宽。(ii)CYP不阻断5HT诱导的或尾部输入诱导的SN体细胞兴奋性增加。(iii)与其对动作电位展宽的阻断同时,CYP可逆地阻断5HT诱导的SNs突触传递促进作用。这些结果表明,内源性释放的5HT可能作用于不同的受体亚型,这些受体亚型与海兔尾部SNs中不同形式的神经调节相关联。

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